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Gillian Reyes-Marcelino

Biographic Data

ID7801747
NAMEGillian Reyes-Marcelino
GIVEN NAMESGillian
FAMILY NAMEReyes-Marcelino
SIGNATUREREYES-MARCELINO G
AFFILIATIONSThe University of Sydney
ORCID0000-0002-3250-0961
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2020
LATEST PUBLICATION YEAR2021
H-INDEX0
  • ‘There is a lot of good in knowing, but there is also a lot of downs’

    Amelia K Smit, Gillian Reyes-Marcelino et al.•ARTICLE•Journal of Medical Ethics•2021

    Publics are key stakeholders in population genomic screening and their perspectives on ethical considerations are relevant to programme design and policy making. Using semi-structured interviews, we explored social views and attitudes towards possible future provision of personalised genomic risk information to populations to inform prevention and/or early detection of relevant conditions. Participants were members of the public (n=30) who had re…

  • Implementation considerations for offering personal genomic risk information to the public

    Open Access•Amelia K Smit, Gillian Reyes-Marcelino et al.•ARTICLE•BMC Public Health•2020

    Participants felt that offering personal genomic risk information to the general population to inform prevention and early detection recommendations is acceptable, particularly for common, complex conditions such as cancer. Understanding participants' preferences for receiving genomic risk information will assist with communication strategies and health workforce planning. We anticipate that these findings will contribute to the development of im…

No prominent works on this page.

  • Implementation considerations for offering personal genomic risk information to the public

    Open Access•Amelia K Smit, Gillian Reyes-Marcelino et al.•ARTICLE•BMC Public Health•2020

    Participants felt that offering personal genomic risk information to the general population to inform prevention and early detection recommendations is acceptable, particularly for common, complex conditions such as cancer. Understanding participants' preferences for receiving genomic risk information will assist with communication strategies and health workforce planning. We anticipate that these findings will contribute to the development of im…

  • ‘There is a lot of good in knowing, but there is also a lot of downs’

    Amelia K Smit, Gillian Reyes-Marcelino et al.•ARTICLE•Journal of Medical Ethics•2021

    Publics are key stakeholders in population genomic screening and their perspectives on ethical considerations are relevant to programme design and policy making. Using semi-structured interviews, we explored social views and attitudes towards possible future provision of personalised genomic risk information to populations to inform prevention and/or early detection of relevant conditions. Participants were members of the public (n=30) who had re…

BRCA gene mutations in cancer (2 works) · Ethics in Clinical Research (2 works) · Medicine (2 works) · Nursing (2 works) · Population (2 works) · Public health (2 works) · Biology (1 work) · Biostatistics (1 work) · Environmental health (1 work) · Genetic testing (1 work)

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